H. Aslam et al., The cycle duration of the seminiferous epithelium remains unaltered duringGnRH antagonist-induced testicular involution in rats and monkeys, J ENDOCR, 161(2), 1999, pp. 281-288
Although the gonadotropic control of the spermatogenic process is well esta
blished, the endocrine regulation of the timing and kinetics of germ cell d
evelopment has received little attention. We found previously that the admi
nistration of a GnRH antagonist (ANT) over a period of 25 days could retard
spermatid development and slightly prolong cycle length in intact adult cy
nomolgus monkeys (Macaca fascicularis). The aim of the present study was to
investigate the effects of extended exposure to ANT on the duration of the
cycle of the seminiferous epithelium in the monkey. Additionally, the dura
tion of spermatogenesis was studied in the ANT-exposed rat model. In experi
ment 1, monkeys were given either saline or ANT (n=6/group) and on day 30 a
ll animals received a single injection of 5-bromodeoxyuridine (BrdU) to lab
el S-phase germ cells. Testicular biopsies were taken on days 39, 43, 17 an
d 51 tend of treatment) for BrdU localization and flow cytometric analysis.
ANT treatment suppressed hormone levels, reduced testis size by >70% and s
everely impaired germ cell production. Despite these alterations, cycle dur
ation remained unchanged at all time-points compared with controls (10.12 /- 0.15 days vs 10.16 +/- 0.44 days). In experiment 2, adult male Sprague-D
awley rats (n=15/group) received either vehicle (VEH) or ANT for 14 days an
d received BrdU injection on day 2. Cycle duration was found to be shorter
in the ANT-treated group (12.45 + 0.09 days) than in the control group (12.
75 +/- 0.08, P<0.05). As spermatogenic cycle length in this control group w
as longer than that of our historical controls (range: 12.37-12.53 days), e
xperiment 2 was repeated (n=10/group). In experiment 3, cycle duration was
12.51+/-0.02 for VEH and 12.46+/-0.05 for the ANT-treated group (P>0.05) in
both species. We concluded that the duration of the cycle of the seminifer
ous epithelium in monkeys and rats is independent of gonadotropins but is r
ather regulated by the spermatogenic tissue itself.